Master Data Specialist

Get AI-powered advice on this job and more exclusive features. Recruitment Manager at Futran Solutions I am Srinivas from Futran Solutions. My client is looking for the below requirement. If you are interested, please reach out to / (609)-945-2335, Ext: 9068 . Job Title: Global Product Development and Supply - Master Data Specialist - 61283-1 Location: Summit, NJ, 07901 - Hybrid (50% onsite) Work Schedule: Mon-Fri (normal business hours) Must Haves: Create, deploy, review, and sustain electronic systems Master Data. Perform data verification, system integration (LIMS, ERP, and MES) for electronic systems. Position Summary: Responsible for the creation and execution of computer system validation documents as well as providing operational support and guidance related to system use and improvement. Duties/Responsibilities: Create and execute computer system validation documents (i.e., UAT, URS, OQ, PQ, etc.) as applicable and guide QC end users on the development of system enhancements with user requirements and business drivers. Provide electronic systems operational support and troubleshooting to end users. Own project, CAPA and deviation/investigation related tasks and/or continuous improvement efforts. Propose and implement improvements to electronic systems to optimize business processes and improve efficiency. Anticipate mid- to long-term business needs and constraints. Support QC management in proposal and implementation of strategic initiatives. Train and mentor others on electronic systems use and operation. Translate business requirements into technical design requirements and communicate to partner organizations (e.g., IT) for system solution. Facilitate design, testing, and subsequent deployment of solutions. Support health agency inspection as equipment area subject matter expert. Perform other tasks as required to support the electronic systems. Reporting Relationship: This position will report to QC management. Qualifications: Specific Knowledge, Skills, Abilities: Ability to accurately and completely understand, follow, interpret, and apply Global Regulatory and cGMP requirements. Ability to work in a fast-paced team environment, meet deadlines, and prioritize work. Advanced technical, problem-solving skills and logical thinking. Ability to communicate effectively with peers, department management, and cross-functional peers. Mentoring, coaching, influencing, negotiating, and personnel interaction skills. Education/Experience/Licenses/Certifications: Bachelor's degree required, preferably in science or related engineering field. 6+ years of relevant work experience in LIMS, ELN, and laboratory data analysis systems preferably in a regulated environment. Knowledge of analytical and microbiological test methods and environmental monitoring programs preferred. Demonstrated technical writing skills. Demonstrated experience with validation and/or maintenance of laboratory information systems. Thanks & Regards, Name: Srinivasa Reddy Mallu. Contact: +1 (609)-945-2335, Ext: 9068 Email Id: Seniority Level: Mid-Senior level Employment Type: Contract Job Function: Analyst, Manufacturing, and Science Industries: Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing #J-18808-Ljbffr

Created: 2025-03-07